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European experience with methotrexate treatment in Crohn's disease: a multicenter retrospective analysis
Uri Kopylov1, Konstantinos H Katsanos, Christien Janneke van der Woude
1aDepartment of Gastroenterology, Sheba Medical Center, Ramat Gan bSackler Medical School, Tel-Aviv University, Tel-Aviv cDepartment of Gastroenterology and Hepatology, Ben-Gurion University of the Negev, Beer Sheva, Israel dDivision of Gastroenterology, University of Ioannina, Ioannina eDepartment of Gastroenterology, Venizeleio General Hospital, Heraklion fFirst Department of Gastroenterology, Evangelismos Hospital, Athens gDepartment of Gastroenterology, University Hospital Heraklion, Crete, Greece hDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, The Netherlands iDepartment of Gastroenterology, Instituto de Investigacion Biomedica Ourense-Pontevedra-Vigo, Xerencia Xestion Integrada de Vigo, Spain jDepartment of Gastroenterology and Hepatology, Zvezdara University Clinical Centre, Zvezdara kMedical Faculty, University of Belgrade, Belgrade, Serbia lCentral IBD Clinic, Nicosia, Cyprus mIBD Center, Department of Gastroenterology, Humanitas Research Hospital, Milan, Italy.
Introduction:
Methotrexate (MTX) has been utilized for the treatment of Crohn's disease (CD) for decades. Nevertheless, current data provide equivocal evidence on the efficacy of MTX in CD.The aims of this study were to describe the efficacy of MTX for maintenance of remission in CD and to identify the factors associated with the probability of steroid-free clinical remission in a multicenter European referral center cohort.
Patients And Methods:
This was a retrospective cohort analysis. Consecutive patients treated with MTX for CD were included from 11 referral centers. Patients receiving concomitant treatment with tumor necrosis factor inhibitors or thiopurines were excluded. The main outcome was steroid-free clinical remission; the secondary outcomes included the rate of complications leading to MTX discontinuation and duration of relapse-free survival in patients achieving the main outcome.
Results:
Between July 1992 and January 2012, 118 patients were identified for inclusion. MTX administration route was oral for induction in 31.4% and for maintenance in 49.1% of the patients. Steroid-free remission was achieved in 44/118 (37.2%) patients and was maintained relapse free by 28/44 (63.6%) for a median of 12 (3.5-18.5) months. At least one adverse effect was reported by 28.9% of the patients. No clinical or demographic factors were associated with either likelihood of achieving a clinical response or duration of relapse-free survival.
Conclusion:
MTX treatment induced steroid-free clinical remission in over a third of CD patients and maintained it for a year in almost two-thirds of the responders. MTX should be considered a viable therapeutic option in CD patients refractory to other therapies.
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